Hydroquinone 8%.
Product Images NDC 72934-6122

3 FDA label images from Sincerus Florida, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydroquinone 8%. (NDC 72934-6122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Fs (2 End)

Fs (2 End)
This image shows the directions for use and contact information panel of a drug container. It includes instructions to apply the medication topically as directed by a physician, to wash hands after use, and to store at controlled room temperature (20-25°C). The label also provides the manufacturer address and phone number for reporting adverse reactions, along with references to FDA MedWatch.*
FDA Label Image

Sf (6122 2 Front)

Sf (6122 2 Front)
HYDROQUINONE USP 8% emulsion in a 30gm white plastic container. The label shows the NDC 72934-6122-2 and is marked as a compounded drug made in the USA. The labeler is Sincerus Florida, LLC, with a logo featuring turquoise and orange colors. The product is marked Rx only with lot number and manufacturing details partially visible.*
FDA Label Image

Sdf (6122 2 Middle)

Sdf (6122 2 Middle)
Label of HYDROQUINONE 8% by Sincerus Florida, LLC, showing the inactive ingredients list. Inactive ingredients include Ascorbyl Palmitate FCC, Citric Acid USP Anhydrous, Cyclomethicone, Dow Corning 1501 and 9011, Edetate Disodium USP Dihydrate, Green Tea Extract, Kojic Acid, Purified Water USP, Sodium Chloride USP, Sodium Metabisulfite NF, and Vitamin E Acetate USP Liquid. The active ingredient is Hydroquinone USP 8%.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.